Top 5 Clinical research associate Jobs in Prairie View Tx

Sub Investigator
DM CLINICAL RESEARCH GROUP —Tomball, TX
- Nursing
- Management
- Patient monitoring

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Clinical Research Coordinator-Clinical Trials Management Office
The Ohio State University Wexner Medical Center —Columbus, OH
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Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Sub Investigator

DM CLINICAL RESEARCH GROUP -
Tomball, TX

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Job Details

Qualifications

Foreign language proficiency
Direct patient care
Nursing
Management
Healthcare staff management
Patient monitoring
Research ethical considerations
EKG
Writing skills
Master's degree in nursing
Assisting with diagnostic tests and procedures
Care documentation
Clinic experience
Mid-level
State healthcare regulations
Patient safety
Master's degree
Data integrity and documentation
ICH guidelines
Collecting samples for laboratory testing
Bachelor's degree
Research safety & compliance
Nurse Practitioner (NP)
Master of Nursing
Managing clinical research teams
Clinical documentation
Research compliance clinical trial records management
Advanced practice provider
Clinical trial standard operating procedures
Clinical trial patient safety management

Full Job Description

The Sub-Investigator is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of subject generated data and directing the conduct of research according to federal and state regulations and guidance documents.

DUTIES & RESPONSIBILITIES

Completing DMCR-required training, including GCP and IATA.
Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
Maintaining a current, up-to-date curriculum vitae and current licensure to practice.
Assisting in managing the activities and performance of the clinical staff affiliated with the site.
Performing clinical-related procedures and/or making important trial-related decisions delegated by the Principal Investigator.
Performing clinical safety assessments and monitoring for study trial participation to include such items as: physical exams, EKGs, phlebotomy, and lab work evaluation
Possessing a thorough understanding of the requirements of each protocol.
Managing the medical care of subjects; protecting the rights and welfare of subjects.
Ensuring documentation of study-related procedures, processes, and events.
Attending investigator meetings as necessary for study participation.
Any other matters as assigned by management

KNOWLEDGE & EXPERIENCE

Education:

Bachelors or Masters in Nursing

Experience:

Previous clinical research experience
Nursing experience in a clinical setting

Credentials:

Current nursing licensure in good standing (Nurse practitioner)

Knowledge and Skills:

Basic clinical and patient care skills
Knowledge of nursing and medical principles and techniques
Clinical research knowledge
Strong communication skills, both written and verbal
Strong diagnostic skills
Ethical and legal healthcare principles in patient care
Proficient communication and comprehension skills both verbal and written in the English language are required.
Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.

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